Methods and Devices for Removal of a Tongue Stabilization Device

ABSTRACT

An airway implant device for maintaining and/or creating an opening in air passageways is disclosed. Methods and devices for removing, the device are also disclosed. Methods of treating airway disorders such as sleep apnea and snoring with the airway implant device are disclosed herein.

CROSS-REFERENCES TO RELATED APPLICATIONS

The present application is a continuation-in-part of U.S. patent application Ser. No. 11/847,271, filed on Aug. 29, 2007, which is a continuation-in-part of U.S. patent application Ser. No. 11/737,107, filed on Apr. 18, 2007, which claims benefit to U.S. Provisional Patent Application No. 60/745,254, filed on Apr. 20, 2006; all of which are incorporated herein by reference in their entireties.

BACKGROUND OF THE INVENTION

Snoring is very common among mammals including humans. Snoring is a noise produced while breathing during sleep due to the vibration of the soft palate and uvula. Not all snoring is bad, except it bothers the bed partner or others near the person who is snoring. If the snoring gets worst overtime and goes untreated, it could lead to apnea.

Those with apnea stop breathing in their sleep, often hundreds of times during the night. Usually apnea occurs when the throat muscles and tongue relax during sleep and partially block the opening of the airway. When the muscles of the soft palate at the base of the tongue and the uvula relax and sag, the airway becomes blocked, making breathing labored and noisy and even stopping it altogether. Sleep apnea also can occur in obese people when an excess amount of tissue in the airway causes it to be narrowed.

In a given night, the number of involuntary breathing pauses or “apneic events” may be as high as 20 to 60 or more per hour. These breathing pauses are almost always accompanied by snoring between apnea episodes. Sleep apnea can also be characterized by choking sensations.

Sleep apnea is diagnosed and treated by primary care physicians, pulmonologists, neurologists, or other physicians with specialty training in sleep disorders. Diagnosis of sleep apnea is not simple because there can be many different reasons for disturbed sleep.

The specific therapy for sleep apnea is tailored to the individual patient based on medical history, physical examination, and the results of polysomnography. Medications are generally not effective in the treatment of sleep apnea. Oxygen is sometimes used in patients with central apnea caused by heart failure. It is not used to treat obstructive sleep apnea.

Continuous positive airway pressure (CPAP) is the most common treatment for sleep apnea. In this procedure, the patient wears a mask over the nose or mouth during sleep, and pressure from an air blower forces air through the air passages. The air pressure is adjusted so that it is just enough to prevent the throat from collapsing during sleep. The pressure is constant and continuous. CPAP prevents airway closure while in use, but apnea episodes return when CPAP is stopped or it is used improperly. Many variations of CPAP devices are available and all have the same side effects such as nasal irritation and drying, facial skin irritation, abdominal bloating, mask leaks, sore eyes, and headaches. Some versions of CPAP devices vary the pressure to coincide with the person's breathing pattern, and other CPAP devices start with low pressure, slowly increasing it to allow the person to fall asleep before the full prescribed pressure is applied.

Dental appliances that reposition the lower jaw and the tongue have been helpful to some patients with mild to moderate sleep apnea or who snore but do not have apnea. A dentist or orthodontist is often the one to fit the patient with such a device.

Some patients with sleep apnea may need surgery. Although several surgical procedures are used to increase the size of the airway, none of them is completely successful or without risks. More than one procedure may need to be tried before the patient realizes any benefits. Some of the more common procedures include removal of adenoids and tonsils (especially in children), nasal polyps or other growths, or other tissue in the airway and correction of structural deformities. Younger patients seem to benefit from these surgical procedures more than older patients.

Uvulopalatopharyngoplasty (UPPP) is a procedure used to remove excess tissue at the back of the throat (tonsils, uvula, and part of the soft palate). The success of this technique may range from 30 to 60 percent. The long-term side effects and benefits are not known, and it is difficult to predict which patients will do well with this procedure.

Laser-assisted uvulopalatoplasty (LAUP) is done to eliminate snoring but has not been shown to be effective in treating sleep apnea. This procedure involves using a laser device to eliminate tissue in the back of the throat. Like UPPP, LAUP may decrease or eliminate snoring but not eliminate sleep apnea itself. Elimination of snoring, the primary symptom of sleep apnea, without influencing the condition may carry the risk of delaying the diagnosis and possible treatment of sleep apnea in patients who elect to have LAUP. To identify possible underlying sleep apnea, sleep studies are usually required before LAUP is performed.

Somnoplasty is a procedure that uses RF to reduce the size of some airway structures such as the uvula and the back of the tongue. This technique helps in reducing snoring and is being investigated as a treatment for apnea.

Tracheostomy is used in persons with severe, life-threatening sleep apnea. In this procedure, a small hole is made in the windpipe and a tube is inserted into the opening. This tube stays closed during waking hours and the person breathes and speaks normally. It is opened for sleep so that air flows directly into the lungs, bypassing any upper airway obstruction. Although this procedure is highly effective, it is an extreme measure that is rarely used.

Patients in whom sleep apnea is due to deformities of the lower jaw may benefit from surgical reconstruction. Surgical procedures to treat obesity are sometimes recommended for sleep apnea patients who are morbidly obese. Behavioral changes are an important part of the treatment program, and in mild cases behavioral therapy may be all that is needed. Overweight persons can benefit from losing weight. Even a 10 percent weight loss can reduce the number of apneic events for most patients. Individuals with apnea should avoid the use of alcohol and sleeping pills, which make the airway more likely to collapse during sleep and prolong the apneic periods. In some patients with mild sleep apnea, breathing pauses occur only when they sleep on their backs. In such cases, using pillows and other devices that help them sleep in a side position may be helpful.

Recently, Restore Medical, Inc., Saint Paul, Minn. has developed a new treatment for snoring and apnea, called the Pillar technique. Pillar System involves a procedure where 3 or more small polyester rod devices are placed in the patient's soft palate. The Pillar System stiffens the palate, reduces vibration of the tissue, and prevents the possible airway collapse. Stiff implants in the soft palate, however, could hinder patient's normal functions like speech, ability to swallow, coughing and sneezing. Protrusion of the implant into the airway is another long-term concern.

As the current treatments for snoring and/or apnea are not effective and have side-effects, there is a need for additional treatment options.

BRIEF SUMMARY OF THE INVENTION

Methods and devices for the treatment of airway disorders, such as snoring and/or apnea are disclosed herein. In another embodiment, the present invention provides an implant for stabilizing the tongue. The implant includes a first anchoring portion for securing a first end of the implant with the mandibula; a control portion connected with the anchoring portion, configured for selectively activating the implant; a flexible portion connected at its proximal end with the control portion, the flexible portion having three-dimensional flexibility in a first state and the flexible portion having a lesser three-dimensional flexibility in a second state, the flexible portion being selectively switchable between the first and second state by the control portion; a second anchoring portion connected with an end of the flexible portion, the second anchoring portion being configured for connecting the implant with the base of the tongue; and a latch mechanism coupled with the control portion and configured to maintain the flexible portion in either of the first and second states.

In one aspect, the implant's first anchoring portion includes an anchoring bracket.

In another aspect, the control portion includes a shape memory member coupled with a flexible fiber, the fiber being connected at its proximal end with the shape memory member and the fiber being connected at its distal end with the distal end of the flexible portion, the flexible fiber being configured to impart an axial load on the flexible portion.

In another aspect, the latch mechanism is a normally closed latch mechanism, wherein the normally closed latch mechanism is configured to securely hold the flexible fiber when the latch mechanism is in a nonpowered state.

In one aspect, the latch mechanism includes a retainer ring coupled with a retainer ring engaging member that is coupled with the flexible fiber.

In another aspect, the latch mechanism also includes a shape memory material connected with the retainer ring. The shape memory material is configured to open the retainer ring when powered to release the retainer ring engaging member.

In another aspect, the latch mechanism includes a spring biased collet configured to securely hold the flexible fiber.

In one aspect, the spring-biased collet latch mechanism also includes a shape memory material connected with the collet, the shape memory material being configured to urge the spring-biased collet away from the collet's biased position when powered to release the flexible fiber from the collet.

In one aspect, the shape memory actuator member is made from a shape memory material configured to transition from a substantially martensitic phase to a substantially austenitic phase beginning at approximately 47 Deg. C.

In another aspect, the shape memory material is configured to experience a contraction when its temperature is elevated above approximately 47 Deg. C. And the shape memory material is configured to experience an expansion after the contraction when its temperature is lowered below approximately 52 Deg. C.

In another aspect, the control portion is powered by a non-implanted inductively coupled power source.

In another aspect, the flexible portion includes a flexible helical spring.

In another aspect, the flexible portion includes a bellows structure.

In another aspect, the flexible portion includes an etched stent-like portion.

In another aspect, the flexible portion is coated with a hyaluronic acid coating.

In another aspect, the second anchoring portion includes a first disc connected with the distal end of the flexible portion and a second disc connectible with the base of the tongue.

In one aspect, the first and second discs include suture holes disposed around their circumferences.

In another aspect, the first and second discs also include polyester rods having holes extending from the flat surfaces of the discs.

In another aspect, the second anchoring portion include a first proximally extending anchor portion and a second distally extending anchor portion.

In one aspect, the control portion includes a microprocessor. The microprocessor being adapted and configured to sense closing of the air passageway and controlling an energizing of the flexible portion.

In another aspect, the tongue implant device also includes a coating to prevent tissue in-growth.

In another aspect, the tongue implant device also includes a coating to promote tissue growth.

In one aspect, the tongue implant device also includes a sensor element, where the sensor is adapted and configured to monitor a condition of an airway to determine likelihood of an apneic event. The condition monitored can be an air passageway gap, air flow pressure, and/or wall tension. The device can also provide feedback to modulate the opening of the air passageway by the flexible portion.

In another embodiment, a method of treating a disease using an airway implant device is disclosed. The method involves implanting in a subject a device having a first anchoring portion for securing a first end of the implant with the mandibula; a control portion connected with the anchoring portion, configured for selectively activating the implant; a flexible portion connected at its proximal end with the control portion, the flexible portion having three-dimensional flexibility in a first state and the flexible portion having a lesser three-dimensional flexibility in a second state, the flexible portion being selectively switchable between the first and second state by the control portion; a second anchoring portion connected with the distal end of the flexible portion, the second anchoring portion being configured for connecting the implant with the base of the tongue; and a latch mechanism coupled with the control portion and configured to maintain the flexible portion in either of the first and second states, the device being adapted and configured to support the tongue upon being energized. The disease can be a sleep disorder. The sleeping disorder can be an obstructive sleep apnea or snoring.

In yet another embodiment, a method is disclosed for removing a previously implanted tongue device, including making a first incision under the chin area to expose the mandible and the implanted device, detaching a proximal portion of the implanted device at a flexible section of the implanted device, the flexible section connected to an anchor in the tongue base, guiding a portion of the flexible section to a cannula of a removal device which is advanced through the first incision, advancing the cannula towards the tongue base, making a second incision in the tongue base through the oral cavity and above the anchors, pushing the cannula through the second incision made in the tongue base and into the oral cavity, and removing the implanted device from the oral cavity.

In one aspect, the method may additionally include collapsing at least a portion of the anchor.

In another aspect, collapsing may be performed using a clamping device.

In another aspect, collapsing may be performed by pulling on at least one suture member which is attached to at least a portion of the anchor.

In another aspect, the suture member may be bioabsorbable.

In another aspect, at least a portion of the anchor may be covered by a cap which allows the anchor to be pushed into the oral cavity.

In another aspect, the cap may be constructed from a biodegradable material.

In another aspect, the method additionally may include visually confirming the implanted device entering the oral cavity.

In another aspect, the cannula of the removal device may include a hypotube which is beveled at a distal portion.

In another aspect, guiding may include attaching a suture to the flexible section and advancing the suture through the cannula of the removal device.

In another aspect, the removal device may apply a tension to the suture.

In another aspect, the removal device may include a suture grasping mechanism inside the cannula.

In another aspect, the suture grasping mechanism may include a loop snare.

In another aspect, the method may include detaching the portion of a previously implanted tongue implant device from the mandible.

In yet another embodiment, a removable implant is disclosed for aiding in stabilizing the tongue, including a control portion which attaches to a mandible, the control portion including a actuator, a flexible portion which connects to a control portion and is actuated by the actuator, an anchoring member connected with the flexible portion, the anchoring member being configured to be implanted within a tongue base, and sutures connected to at least a portion of the anchoring member and extending to the control portion, which when pulled collapses at least a portion of the anchoring member.

In one aspect, the tongue anchoring portion may include hooks and the sutures are looped around the hooks.

In another, aspect the removable implant may additionally include a cap positioned about a portion of the anchoring member.

In another, aspect the cap is bioabsorbable.

In another, aspect the removable implant may additionally include a bracket attached to the control portion, and configured to anchor to a mandible.

In another, aspect the removable implant may additionally include a bioabsorbable sheath surrounding the flexible portion.

In another, aspect the sutures may be bioabsorbable.

In yet another embodiment, a method is disclosed for removing a previously implanted tongue implant device, including creating an incision about the mandible area where a portion of a previously implanted tongue implant device is attached to the mandible, detaching the portion of a previously implanted tongue implant device from the mandible, the previously implanted tongue device also including anchors secured to the tongue, remotely collapsing at least a portion of the anchors of the previously implanted tongue device and pulling out the previously implanted tongue device through the incision.

In one aspect, the previously implanted tongue implant device may be located within a sheath.

In another aspect, the method may additionally include pulling the sheath out of the incision.

In another aspect, collapsing may be performed using a clamping device.

In another aspect, collapsing may be performed by pulling on at least one suture member which is attached to least a portion of the anchor.

In another aspect, the suture member may be bioabsorbable.

In another aspect, the method may additionally include inserting a removal device into the incision and using the removal device for pulling out the previously implanted tongue device.

In another aspect, the removal device may include a hypotube which is beveled at a distal portion.

In another aspect, the removal device may snare a portion of the previously implanted tongue implant device.

In another aspect, the previously implanted tongue implant device may not have been implanted for a long enough period for tissue to significantly adhere to the previously implanted tongue implant device.

For a further understanding of the nature and advantages of the invention, reference should be made to the following description taken in conjunction with the accompanying figures. It is to be expressly understood, however, that each of the figures is provided for the purpose of illustration and description only and is not intended as a definition of the limits of the embodiments of the present invention.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 illustrates one embodiment of the airway implant device.

FIG. 2 illustrates one embodiment of the airway implant device.

FIG. 3 illustrates one embodiment of the airway implant device.

FIG. 4 illustrates one embodiment of the airway implant device.

FIG. 5 illustrates a circuit diagram of an embodiment of the airway implant device.

FIG. 6 illustrates an embodiment of the airway implant device.

FIG. 7 illustrates a sectional view of an embodiment of the electroactive polymer element.

FIG. 8 illustrates a sectional view of an embodiment of the electroactive polymer element.

FIG. 9 illustrates an embodiment of the electroactive polymer element.

FIG. 10 illustrates an embodiment of the electroactive polymer element.

FIG. 11 illustrates an embodiment of the electroactive polymer element.

FIG. 12 illustrates an embodiment of the electroactive polymer element.

FIG. 13 illustrates an embodiment of the electroactive polymer element.

FIG. 14 illustrates an embodiment of the electroactive polymer element.

FIG. 15 illustrates an embodiment of the electroactive polymer element.

FIG. 16 illustrates an embodiment of the electroactive polymer element.

FIG. 17 illustrates an embodiment of the electroactive polymer element.

FIG. 18 illustrates an embodiment of the electroactive polymer element.

FIG. 19 illustrates an embodiment of the electroactive polymer element.

FIG. 20 illustrates an embodiment of the implanted portion of the airway implant device.

FIG. 21 illustrates an embodiment of the airway implant device.

FIG. 22 illustrates an embodiment of the non-implanted portion in the form of a mouth guard.

FIG. 23 illustrates an embodiment of the non-implanted portion in the form of a mouth guard.

FIG. 24 illustrates an embodiment of the non-implanted portion.

FIG. 25 shows a sagittal section through a head of a subject illustrating an embodiment of a method for using the airway implant device.

FIG. 26 illustrates an anterior view of the mouth with see-through mouth roofs to depict an embodiment of a method for using the airway implant device.

FIG. 27 illustrates an anterior view of the mouth with see-through mouth roofs to depict an embodiment of a method for using the airway implant device.

FIG. 28 illustrates an anterior view of the mouth with see-through mouth roofs to depict an embodiment of a method for using the airway implant device.

FIG. 29 illustrates an anterior view of the mouth with see-through mouth roofs to depict an embodiment of a method for using the airway implant device.

FIG. 30 illustrates an embodiment of an inductive coupling system associated with the airway implant device.

FIG. 31 illustrates an embodiment of the airway implant device.

FIG. 32 illustrates an embodiment of the airway implant device.

FIG. 33 illustrates an embodiment in which a patient wears the non-implanted portion of the device on the cheeks.

FIG. 34A-34B illustrates an embodiment of a method of the invention with the airway implant in the soft palate.

FIG. 35A-35B illustrates an embodiment of a method of the invention with the airway implants in the soft palate and lateral pharyngeal walls.

FIG. 36A-36B illustrates an embodiment of a method of the invention with the airway implants in the lateral pharyngeal walls.

FIG. 37 depicts the progression of an apneic event.

FIG. 38 depicts an embodiment of an airway implant device with sensors in the soft palate and laryngeal wall.

FIG. 39 depicts the functioning of an airway implant device with sensors in the soft palate and laryngeal wall.

FIG. 40 depicts an embodiment of an airway implant device with a sensor in the laryngeal wall.

FIG. 41 depicts an example of controller suitable for use with an airway implant device.

FIG. 42 depicts an embodiment of an airway implant device.

FIG. 43A depicts an embodiment of an airway implant device.

FIG. 43B depicts an embodiment of the non-implantable portion of the airway implant device of FIG. 43A.

FIG. 44 depicts an embodiment of an airway implant device.

FIG. 45A-D depicts an embodiment of the deformable element.

FIG. 46 is a simplified drawing of an exemplary tongue implant device in accordance with one embodiment of the present invention shown implanted in the tongue.

FIG. 47 is photograph of an exemplary prototype tongue implant device in accordance with one embodiment of the present invention.

FIG. 48 is a simplified schematic drawing of an exemplary tongue implant device in accordance with another embodiment of the present invention.

FIG. 49 is a simplified schematic drawing of an exemplary tongue implant device in accordance with another embodiment of the present invention.

FIG. 50 illustrates the overall appearance of the implant of FIG. 49.

FIGS. 51A-D illustrate one exemplary procedure for the placement of the tongue implant.

FIG. 52 illustrates one embodiment of the latch mechanism for the tongue implant.

FIG. 53 is a simplified drawing illustrating an exemplary tongue implant device in accordance with another embodiment of the present invention (the proximal bracket portion is not shown).

FIG. 54 is an exploded assembly view drawing corresponding to the implant of FIG. 53.

FIG. 55A illustrates the collet latch in its normally-closed position, and FIG. 55B shows the collet latch in its open position.

FIG. 56 is a graph of the performance characteristic for the shape memory actuator material used in the tongue implant.

FIG. 57A is a simplified drawing of an exemplary tongue implant device, in accordance with one embodiment of the present invention.

FIGS. 57B-E are partial cross-sectional views illustrating a method for removing a previously implanted exemplary tongue device, in accordance with one embodiment of the present invention.

FIG. 58A is a simplified drawing of an exemplary tongue implant device, in accordance with one embodiment of the present invention.

FIGS. 58B-C are partial cross-sectional views illustrating a method for removing a previously implanted exemplary tongue device, in accordance with one embodiment of the present invention.

FIG. 59A is a top view of a removal device, in accordance with one embodiment of the present invention.

FIG. 59B is a perspective view of a clamping device, in accordance with one embodiment of the present invention.

DETAILED DESCRIPTION OF THE INVENTION Devices and Methods

A first aspect of the invention is a device for the treatment of disorders associated with improper airway patency, such as snoring or sleep apnea. The device comprises of a deformable element to adjust the opening of the airway. In a preferred embodiment, the deformable element comprises of an electroactive polymer (EAP) element. The electroactive polymer element in the device assists in maintaining appropriate airway opening to treat the disorders. Typically, the EAP element provides support for the walls of an airway, when the walls collapse, and thus, completely or partially opens the airway.

The device functions by maintaining energized and non-energized configurations of the EAP element. In preferred embodiments, during sleep, the EAP element is energized with electricity to change its shape and thus modify the opening of the airway. Typically, in the non-energized configuration the EAP element is soft and in the energized configuration is stiffer. The EAP element of the device can have a pre-set non-energized configuration wherein it is substantially similar to the geometry of the patient's airway where the device is implanted.

In some embodiments, the device, in addition to the EAP element, includes an implantable transducer in electrical communication with the EAP element. A conductive lead connects the EAP element and the implantable transducer to the each other. The device of the present invention typically includes a power supply in electrical communication with the EAP element and/or the implantable transducer, such as a battery or a capacitor. The battery can be disposable or rechargeable.

Preferred embodiments of the invention include a non-implanted portion, such as a mouthpiece, to control the implanted EAP element. The mouthpiece is typically in conductive or inductive communication with an implantable transducer. In one embodiment, the mouthpiece is a dental retainer with an induction coil and a power source. The dental retainer can further comprise a pulse-width-modulation circuit. When a dental retainer is used it is preferably custom fit for the individual biological subject. If the implantable transducer is in inductive communication, it will typically include an inductive receiver, such as a coil. The implantable transducer can also include a conductive receiver, such as a dental filling, a dental implant, an implant in the oral cavity, an implant in the head or neck region. In one embodiment, the device includes a dermal patch with a coil, circuit and power source, in communication with the implantable transducer. The dermal patch can also include a pulse-width-modulation circuit.

Another aspect of the invention is a method to modulate air flow through airway passages. Such modulation is used in the treatment of diseases such as snoring and sleep apnea. One method of the invention is a method for modulating the airflow in airway passages by implanting in a patient a device comprising a deformable element and controlling the device by energizing the deformable element. The deformable element preferably comprises an electroactive polymer element. The deformable element can be controlled with a mouthpiece inserted into the mouth of the patient. The energizing is typically performed with the use of a power supply in electrical communication, either inductive communication or conductive communication, with the deformable element. A transducer can be used to energize the deformable element by placing it in electrical communication with the power supply. Depending on the condition being treated, the deformable element is placed in different locations such as soft palate, airway sidewall, uvula, pharynx wall, trachea wall, larynx wall, and/or nasal passage wall.

A preferred embodiment of the device of the present invention comprises an implantable deformable element; an implantable transducer; an implantable lead wire connecting the deformable element and the transducer; a removable transducer; and a removable power source; and wherein the deformable element comprises an electroactive polymer.

Electroactive polymer is a type of polymer that responds to electrical stimulation by physical deformation, change in tensile properties, and/or change in hardness. There are several types of electroactive polymers like dielectric electrostrictive polymer, ion exchange polymer and ion exchange polymer metal composite (IPMC). The particular type of EAP used in the making of the disclosed device can be any of the aforementioned electroactive polymers.

Suitable materials for the electroactive polymer element include, but are not limited to, an ion exchange polymer, an ion exchange polymer metal composite, an ionomer base material. In some embodiments, the electroactive polymer is perfluorinated polymer such as polytetrafluoroethylene, polyfluorosulfonic acid, perfluorosulfonate, and polyvinylidene fluoride. Other suitable polymers include polyethylene, polypropylene, polystyrene, polyaniline, polyacrylonitrile, cellophane, cellulose, regenerated cellulose, cellulose acetate, polysulfone, polyurethane, polyvinyl alcohol, polyvinyl acetate, polyvinyl pyrrolidone. Typically, the electroactive polymer element includes a biocompatible conductive material such as platinum, gold, silver, palladium, copper, and/or carbon.

Suitable shapes of the electroactive polymer element include three dimensional shape, substantially rectangular, substantially triangular, substantially round, substantially trapezoidal, a flat strip, a rod, a cylindrical tube, an arch with uniform thickness or varying thickness, a shape with slots that are perpendicular to the axis, slots that are parallel to the longitudinal axis, a coil, perforations, and/or slots.

IPMC is a polymer and metal composite that uses an ionomer as the base material. Ionomers are types of polymers that allow for ion movement through the membrane. There are several ionomers available in the market and some of the suited ionomers for this application are polyethylene, polystyrene, polytetrafluoroethylene, polyvinylidene fluoride, polyfluorosulfonic acid based membranes like NAFION® (from E. I. Du Pont de Nemours and Company, Wilmington, Del.), polyaniline, polyacrylonitrile, cellulose, cellulose acetates, regenerated cellulose, polysulfone, polyurethane, or combinations thereof. A conductive metal, for example gold, silver, platinum, palladium, copper, carbon, or combinations thereof, can be deposited on the ionomer to make the IPMC. The IPMC element can be formed into many shapes, for example, a strip, rod, cylindrical tube, rectangular piece, triangular piece, trapezoidal shape, arch shapes, coil shapes, or combinations thereof. The IPMC element can have perforations or slots cut in them to allow tissue in growth.

The electroactive polymer element has, in some embodiments, multiple layers of the electroactive polymer with or without an insulation layer separating the layers of the electroactive polymer. Suitable insulation layers include, but are not limited to, silicone, polyurethane, polyimide, nylon, polyester, polymethylmethacrylate, polyethylmethacrylate, neoprene, styrene butadiene styrene, or polyvinyl acetate.

In some embodiments, the deformable element, the entire device, or portions of the airway implant have a coating. The coating isolates the coated device from the body fluids and/or tissue either physically or electrically. The device can be coated to minimize tissue growth or promote tissue growth. Suitable coatings include poly-L-lysine, poly-D-lysine, polyethylene glycol, polypropylene, polyvinyl alcohol, polyvinylidene fluoride, polyvinyl acetate, hyaluronic acid, and/or methylmethacrylate.

Embodiments of the Device

FIG. 1 illustrates an airway implant system 2 that has a power supply 4, a connecting element, such as a wire lead 14, and a deformable element, such as an electroactive polymer element 8. Suitable power supplies 4 are a power cell, a battery, a capacitor, a substantially infinite bus (e.g., a wall outlet leading to a power generator), a generator (e.g., a portable generator, a solar generator, an internal combustion generator), or combinations thereof. The power supply 4 typically has a power output of from about 1 mA to about 5 A, for example about 500 mA.

Instead of or in addition to wire lead 14, the connecting element may be an inductive energy transfer system, a conductive energy transfer system, a chemical energy transfer system, an acoustic or otherwise vibratory energy transfer system, a nerve or nerve pathway, other biological tissue, or combinations thereof. The connecting element is made from one or more conductive materials, such as copper. The connecting element is completely or partially insulated and/or protected by an insulator, for example polytetrafluoroethylene (PTFE). The insulator can be biocompatible. The power supply 4 is typically in electrical communication with the deformable element 8 through the connecting element. The connecting element is attached to an anode 10 and a cathode 12 on the power supply 4. The connecting elements can be made from one or more sub-elements.

The deformable element 8 is preferably made from an electroactive polymer. Most preferably, the electroactive polymer is an ion exchange polymer metal composite (IPMC). The IPMC has a base polymer embedded, or otherwise appropriately mixed, with a metal. The IPMC base polymer is preferably perfluoronated polymer, polytetrafluoroethylene, polyfluorosulfonic acid, perfluorosulfonate, polyvinylidene fluoride, hydrophilic polyvinylidene fluoride, polyethylene, polypropylene, polystyrene, polyaniline, polyacrylonitrile, cellophane, cellulose, regenerated cellulose, cellulose acetate, polysulfone, polyurethane, polyvinyl alcohol, polyvinyl acetate and polyvinyl pyrrolidone, or combinations thereof. The IPMC metal can be platinum, gold, silver, palladium, copper, carbon, or combinations thereof.

FIG. 2 illustrates that the deformable element 8 can have multiple elements 8 and connecting elements 14 that all connect to a single power supply 4.

FIG. 3 illustrates an airway implant system 2 with multiple power supplies 4 and connecting elements 14 that all connect to a single deformable element 8. The airway implant system 2 can have any number and combination of deformable elements 8 connected to power supplies 4.

FIG. 4 illustrates an embodiment with the connecting element having a first energy transfer element, for example a first transducer such as a first receiver, and a second energy transfer element, for example a second transducer such as a second inductor 16. In this embodiment, the first receiver is a first inductor 18. The first inductor 18 is typically positioned close enough to the second inductor 16 to enable sufficient inductive electricity transfer between the second and first inductors 16 and 18 to energize the deformable element 8. The connecting element 14 has multiple connecting elements 6.

FIG. 5 illustrates that the airway implant device of the present invention can have an implanted portion 20 and a non-implanted portion 22. In this embodiment, the implanted portion 20 is a closed circuit with the first inductor 18 in series with a first capacitor 24 and the deformable element 8. The deformable element 8 is attached to the closed circuit of the implanted portion 20 by a first contact 26 and a second contact 28. In some embodiments, the implanted portion has a resistor (not shown). The non-implanted portion 22 is a closed circuit. The non-implanted portion 22 has a second inductor 16 that is in series with a resistor 30, the power supply 4, and a second capacitor 32. The capacitors, resistors, and, in-part, the inductors are representative of the electrical characteristics of the wire of the circuit and not necessarily representative of specific elements. The implanted portion 20 is within tissue and has a tissue surface 33 nearby. The non-implanted portion is in an insulation material 35. An air interface 37 is between the tissue surface 33 and the insulation material 35.

FIG. 6 illustrates an embodiment in which the first energy transfer element of the connecting element 14 is a first conductor 34. The second energy transfer element of the connecting element 14 is a second conductor 36. The first conductor 34 is configured to plug into, receive, or otherwise make secure electrical conductive contact with the second conductor 36. The first conductor 34 and/or second conductor 36 are plugs, sockets, conductive dental fillings, tooth caps, fake teeth, or any combination thereof.

FIG. 7 illustrates an embodiment in which the deformable element 8 is a multi-layered device. The deformable element 8 has a first EAP layer 38, a second EAP layer 40, and a third EAP layer 42. The EAP layers 38, 40 and 42 are in contact with each other and not separated by an insulator.

FIG. 8 illustrates another embodiment in which the deformable element 8 has a first EAP layer 38 separated from a second EAP layer 40 by a first insulation layer 44. A second insulation layer 46 separates the second EAP layer from the third EAP layer 42. A third insulation layer 48 separates the third EAP layer from the fourth EAP layer 50. Insulation material is preferably a polymeric material that electrically isolates each layer. The insulation can be, for example, acrylic polymers, polyimide, polypropylene, polyethylene, silicones, nylons, polyesters, polyurethanes, or combinations thereof. Each EAP layer, 38, 40, 42 and 50 can be connected to a lead wire (not shown). All anodes and all cathodes are connected to the power supply 4.

FIGS. 9-19 illustrate different suitable shapes for the deformable element 8. FIG. 9 illustrates a deformable element 8 with a substantially flat rectangular configuration. The deformable element 8 can have a width from about 2 mm to about 5 cm, for example about 1 cm. FIG. 10 illustrates a deformable element 8 with an “S” or zig-zag shape. FIG. 11 illustrates the deformable element 8 with an oval shape. FIG. 12 illustrates a deformable element 8 with a substantially flat rectangular shape with slots 52 cut perpendicular to the longitudinal axis of the deformable element 8. The slots 52 originate near the longitudinal axis of the deformable element 8. The deformable element 8 has legs 54 extending away from the longitudinal axis. FIG. 13 illustrates a deformable element 8 with slots 52 and legs 54 parallel with the longitudinal axis. FIG. 14 illustrates a deformable element be configured as a quadrilateral, such as a trapezoid. The deformable element 8 has chamfered corners, as shown by radius. FIG. 15 illustrates a deformable element 8 with apertures 55, holes, perforations, or combinations thereof. FIG. 16 illustrates a deformable element 8 with slots 52 and legs 54 extending from a side of the deformable element 8 perpendicular to the longitudinal axis. FIG. 17 illustrates a deformable element 8 with a hollow cylinder, tube, or rod. The deformable element has an inner diameter 56. FIG. 18 illustrates an arched deformable element 8. The arch has a radius of curvature 57 from about 1 cm to about 10 cm, for example about 4 cm. The deformable element 8 has a uniform thickness. FIG. 19 illustrates an arched deformable element 8. The deformable element 8 can have a varying thickness. A first thickness 58 is equal or greater than a second thickness 60.

FIG. 20 illustrates an embodiment of the implanted portion of an airway implant with a coil-type inductor 18 connected by a wire lead 6 to the deformable element 8. In another embodiment, as illustrated in FIG. 21 the implanted portion has a conductive dental filling 62 in a tooth 64. The dental filling 62 is previously implanted for reasons related or unrelated to using of the airway implant system. The dental filling 62 is electrically connected to the wire lead 6. For example, a portion of the wire lead 6 is implanted in the tooth 64, as shown by phantom line. The wire lead 6 is connected to the deformable element 8.

FIG. 22 illustrates an embodiment of the non-implanted portion 22 with a mouthpiece, such as a retainer 66. The retainer 66 is preferably custom configured to fit to the patient's mouth roof, or another part of the patient's mouth. The second transducer, such as second inductor 16, is integral with, or attached to, the retainer 66. The second inductor 16 is located in the retainer 66 so that during use the second inductor 16 is proximal with the first inductor 18. The power supply 4, such as a cell, is integral with, or attached to, the retainer 66. The power supply 4 is in electrical communication with the second inductor 16. In some embodiments, the retainer 66 has a pulse-width-modulation circuit. FIG. 23 illustrates that the retainer 66 has one or more tooth sockets 68. The tooth sockets 68 are preferably configured to receive teeth that have dental fillings. The tooth sockets 68 are electrically conductive in areas where they align with dental fillings when in use. The power supply 4 is connected with the tooth sockets 68 via the wire leads 6. In the embodiment of FIG. 24, the non-implantable portion 22 has the second inductor 16 attached to a removably attachable patch 70. The patch 70 is attached to the power supply 4. The power supply 4 is in contact with the second inductor 16. This embodiment can be, for example, located on the cheeks as shown on FIG. 33 or any other suitable location.

Preferably, the airway implant device 2 discussed herein is used in combination with an inductive coupling system 900 such as depicted in FIG. 30. FIG. 30 depicts an inductive coupling system that is suitable for controlling the airway implant device 2 which includes a connecting element 906 (which connects the electrical contacts (not shown) to the rest of the electrical system), a connector 901, a energy source 322, a sensor 903, a timer 904, and a controller 905. The connector 901, energy source 322, sensor 903, a timer 904, and controller 905 are located in a housing disposed in a region outside or inside the body.

Two preferred embodiments of the airway implant device are shown in FIGS. 31 and 32. The device in FIG. 31 includes the deformable element 8 connected to an anode 10 and cathode 12 and to the induction coil 18. The device also includes a controller 90, such as a microprocessor. The circuitry within the controller is not shown. The controller 90 picks up AC signals from the induction coil 18 and converts it to DC current. The controller 90 can also include a time delay circuit and/or a sensor. The sensor could sense the collapsing and/or narrowing of the airways and cause the device to energize the deformable element 8 and thus completely or partially open up the airway in which the device is implanted. FIG. 32 shows an embodiment with anchors 91 located on the deformable element 8. The implant can be anchored in a suitable location with the use of these anchors and sutures and/or surgical glue.

FIG. 42 depicts an embodiment of the invention. The airway implant device comprises of two units—an implant unit and a retainer unit. The implant unit is implanted in a patient and includes an IPMC actuator and a coil. The retainer unit is typically not implanted in the patient and can be worn by the patient prior to going to bed. This unit includes a coil, a battery, and a microcontroller.

FIG. 43A-B depicts yet another embodiment of the invention. FIG. 43A is the implant unit, preferably for implantation proximal to or in an airway wall. The implant unit includes a deformable element 8, an inductor 18 in the form of a coil, a controller 90, and connecting elements 6. FIG. 43B depicts the removable retainer with an inductor 16 and a retainer 66.

The implants described herein are preferably implanted with a deployment tool. Typically, the implantation involves an incision, surgical cavitation, and/or affixing the implant.

Sensing and Actuation of Airway Implants

One embodiment of the invention is an airway implant device with a sensor for monitoring a condition prior to and/or during the occurrence of an apneic event. Preferably, the sensor monitors for blockage of an airway. The sensor senses the possible occurrence of an apneic event. This sensing of a possible apneic event is typically by sensing a decrease in the airway gap, a change in air pressure in the airway, or a change in air flow in the airway. A progressive decrease in the airway gap triggers the occurrence of an apneic event. Most preferably the sensor senses one or more events prior to the occurrence an apneic event and activates the airway implant to prevent the apneic event. In some embodiments, the airway implant device and the sensor are in the same unit. In other embodiments, the deformable element of the airway implant device is the sensor. In these embodiments, the deformable element acts as both a sensor and actuator. In yet other embodiments, the airway implant device and the sensor are in two or more separate units.

FIG. 37 depicts the occurrence of an apneic event due to the blockage of airway 3701 caused by the movement of the soft palate 84. FIG. 37A shows the soft palate 84 position during normal breathing cycle. An airway gap 3803 is maintained between the soft palate 84 and the laryngeal wall 3804 to maintain airflow 3805. FIG. 37B shows the position of the soft palate 84 just prior to the airway 3701 blockage. It can be seen that the gap 3803′ in this case is smaller than the gap 3803 in FIG. 37A. FIG. 37C shows the soft palate 84 blocking the airway 3701′, leading to the occurrence of an apneic event. In one aspect of the invention, the event shown in FIG. 37C is prevented by taking preemptive action during occurrence of event depicted in FIG. 37B.

One aspect of the invention is an airway implant device with a sensor for sensing the occurrence of apneic events and actuating the device. The invention also includes methods of use of such device.

One embodiment of an airway implant device with sensor is depicted in FIG. 38. Non-contact distance sensors 3801 and 3802 are mounted on the laryngeal wall 3804 and also on the soft palate 84 to sense the airway gap between the soft palate 84 and the laryngeal wall 3804. One or more gap values are calibrated into a microcontroller controlling the airway implant device. The functioning of the airway implant device with a sensor is depicted in FIG. 39. During the occurrence of the apneic event the gap between the soft palate 84 and the laryngeal wall 3804 decreases. This gap information is continuously monitored by the airway implant device microcontroller. When the gap becomes smaller than a preset threshold value, the airway implant microcontroller actuates the airway implant, which stiffens the soft palate 84 and the gap between the soft palate 84 and the laryngeal walls 3804 increases. When this gap crosses an upper threshold, the microcontroller powers off the airway implant actuator.

In one embodiment, the operation of the device is as follows:

a) A threshold gap is calibrated into the microcontroller which is present in the removable retainer of the device. This threshold gap corresponds to the gap 3803′ formed by the position of the soft palate with respect to the laryngeal wall as depicted in the FIG. 37B, i.e., a distance at which an apneic event could be triggered or an apneic event occurs. This calibration can take place in real time or when the device is being installed. b) The non-contact sensor constantly monitors the gap and the information is constantly analyzed by a program present in the microcontroller. c) The airway implant actuator is in the off state (not powered state) as long as the threshold gap is not reached. d) When the gap is equal to the threshold gap, the micro controller, powers on the airway implant actuator (on state). This leads to the stiffening of the airway implant actuator, which in-turn stiffens the soft palate. e) This stiffening of the soft palate prevents the obstruction of the airway and modulates the occurrence of an apneic event. f) When the gap becomes more than the threshold gap, the micro-controller turns off the airway implant actuator (off state).

Typically, an algorithm in the micro-controller controls the actuation of the actuator. An example of the algorithm is—

-   -   if (gap<threshold gap); {Voltage applied to airway implant         actuator=high (on state)} or else {Voltage applied to the airway         implant actuator=low (off state)}

Complex algorithms, such as adaptive algorithms, can also be used. The objective of the adaptive algorithm can be to selectively control the stiffness of the soft palate by varying the power applied to the airway implant actuator.

Another example of an algorithm to selectively control the stiffness of the soft palate is:

-   -   If (gap<or =g)     -   {Apply full power to the airway implant actuator}     -   Else     -   If (gap=g1)     -   {Voltage applied to airway implant actuator=v}     -   Else if (gap=g2)     -   {Voltage applied to airway implant actuator=v2}     -   Else if (gap=g3)     -   {Voltage applied to airway implant actuator=v3}     -   Note (g1, g2, g3>g)

An example of a controller to maintain a predetermined reference gap is shown is FIG. 41. The objective of this algorithm is to maintain an actual airway gap g_(act) as close to the reference airway gap g_(ref) as possible by controlling the airway implant device actuator. The actual airway gap between the soft palate and the laryngeal wall g_(act) is measured and this information is the output of the position sensor. This airway gap information is feedback to the microcontroller which has a controller algorithm embedded in it. In the microcontroller the g_(act) is compared to a g_(ref) and based on the difference between both, the Proportional Integral Derivative (PID) controller generates a controlling voltage which is supplied to the airway implant device. The PID controller can have fixed gains or can have the gains adaptively tuned based on system information.

In alternative embodiments, the sensor can be a wall tension sensor, an air pressure sensor, or an air flow monitoring sensor. In another embodiment, instead of fully turning the airway implant actuator on or off, the actual value of the airway gap can be used to selectively apply varying voltage to the airway implant actuator, hence selectively varying the stiffness of the soft palate. In yet another embodiment, if the airway implant actuator exhibits a lack of force retention over an extended period of time under DC voltage, a feedback control algorithm may be implemented in the microcontroller, which uses the sensory information provided by the sensors to control the stiffness of the soft palate by maintaining the force developed by the airway implant actuator.

Another embodiment of the invention is depicted in FIG. 40. In this embodiment, the wall tension sensed by the wall tension sensor 4001 implanted into the laryngeal wall 3804 is used as a threshold criterion for activating the airway implant actuator. A wall tension sensor can also be placed in a pharyngeal wall or other suitable airway wall. The sensors of this invention can be placed in an airway wall or proximal to an airway wall.

Some of the advantages of the use of an airway sensor with an airway implant device include: optimization of the power consumed by the airway implant device and hence extension of the life of the device; assistance in predicting the occurrence of apneic event, and hence selective activation of the device in order to minimize any patient discomfort; flexibility to use a feedback control system if required to compensate for any actuator irregularities; and possible configuration of the system to interact with an online data management system which will store different parameters related to apneic events for a patient. This system can be accessed by the doctor, other health care providers, and the insurance agency which will help them provide better diagnosis and understanding of the patient's condition.

In preferred embodiments, the airway gap is individually calculated and calibrated for each patient. This information can be stored in the microcontroller. The sensors are described herein mainly in the context of airway implant devices comprising of electroactive polymer actuators. The sensors can also be used with airway implant devices comprising other active actuators, i.e., actuators that can be turned on, off, or otherwise be controlled, such as magnets. The sensors can be used to activate, in-activate, and/or modulate magnets used in airway implant devices. Preferably, the sensors are in the form of a strip, but can be any other suitable shape for implantation. They are typically deployed with a needle with the help of a syringe. The sensor can be made with any suitable material. In preferred embodiments, the sensor is a smart material, such as an IPMC. The sensor is typically in connection with a microcontroller, which is preferably located in the retainer. This connection can be either physical or wireless.

Suitable sensors include, but are not limited to, an electroactive polymer like ionic polymer metal composite (IPMC). Suitable materials for IPMC include perfluorinated polymer such as polytetrafluoroethylene, polyfluorosulfonic acid, perfluorosulfonate, and polyvinylidene fluoride. Other suitable polymers include polyethylene, polypropylene, polystyrene, polyaniline, polyacrylonitrile, cellophane, cellulose, regenerated cellulose, cellulose acetate, polysulfone, polyurethane, polyvinyl acetate. Typically, the electroactive polymer element includes a biocompatible conductive material such as platinum, gold, silver, palladium, copper, and/or carbon. Commercially available materials suitable for use as a sensor include Nafion® (made by DuPont), Flemion® (made by Asahi Glass), Neosepta® (made by Astom Corporation), Ionac® (made by Sybron Chemicals Inc), Excellion™ (made by Electropure). Other materials suitable for use as a sensor include materials with piezoelectric properties like piezoceramics, electrostrictive polymers, conducting polymers, materials which change their resistance in response to applied strain or force (strain gauges) and elastomers.

The airway implant devices of the present invention, with or without the sensor, can be used to treat snoring. For snoring, the sensor can be adapted and configured to monitor air passageways so as to detect the possible occurrence of snoring or to detect the possible worsening of ongoing snoring. Preferably the sensors are capable of detecting relaxation of tissues in the throat, which can cause them to vibrate and obstruct the airway. Other tissues that can be monitored by the sensor include the mouth, the soft palate, the uvula, tonsils, and the tongue.

Another disease that can be treated with the devices of the present invention includes apnea. The sensor preferably monitors the throat tissue for sagging and/or relaxation to prevent the occurrence of an apneic event. Other tissues that can be monitored by the sensor include the mouth, the soft palate, the uvula, tonsils, and the tongue.

Airway Implant Device

One aspect of the invention is an airway implant device with a connecting element. Preferably the connecting element is used to anchor and/or support the airway implant device, in particular, the deformable element to a rigid structure, such as a bony structure. The invention also includes methods of treating a disease using an airway implant device by implanting in a subject the airway implant device having a deformable element and a connecting element, the implanting step including fastening the deformable element to a bony structure of the subject with the connecting element, wherein the deformable element is capable of modulating the opening of the air passageway. Another method is a method of treating a disease using an airway implant device by implanting a deformable element in a tongue of a subject and linking the deformable element to a jaw bone, the deformable element is capable of supporting the tongue when it is energized. The devices are used to treat sleeping disorders, such as obstructive sleep apnea or snoring.

One embodiment is an airway implant device having a deformable element and a connecting element, wherein the deformable element is capable of modulating the opening of an air passageway and the connecting element is used to fasten the deformable element to a rigid structure. Preferably, the rigid structure is a bony structure. The deformable element can be made of a magnetic material or an electroactive polymer element. In some embodiments, both the deformable element and connecting element are made from a polymeric material. In this embodiment, the polymeric material of the deformable element is typically an electroactive polymer. The electroactive polymer element can include an ion-exchange polymer metal composite. In other embodiments, the electroactive polymer element can include a conducting polymer such as a polypyrrole, a carbon nanotube or a polyaniline.

One embodiment of the airway implant device with a connecting element is depicted in FIG. 44. The deformable element 8 is linked to the jaw bone with a connecting element 4401. A first inductor 18 is implanted in the patient and a second inductor 16 is located on the outside and can be worn by the patient when the airway implant device needs to be activated, for example prior to going to sleep.

The deformable element can have a suitable shape such as a flat surface or a tube. Preferably, the deformable element is adapted and configured to expand and contract like an accordion, in particular for an airway implant device that is used for implantation in the tongue. Examples of shapes of the deformable element 8 are depicted in FIG. 45A-45D. These forms are particularly useful for implantation in the tongue. FIG. 45A depicts a deformable element 8 with a single layer 4501 of suitable material, such as an electroactive polymer or a magnetic material, with folds 4502. FIG. 45B depicts a deformable element 8 with two layers 4501 and 4501′, joined by layers 4503 and 4503′ and folds 4502 and 4502′. FIG. 45C depicts a deformable element 8 with a series of layers 4504 which are connected to each other with a connecting element 4506. The connecting element 4506 allows the layers 4504 to slide along its length. The connecting element 4506 and the layers 4504 can be made of the same material or different materials. FIG. 45D depicts a deformable element 8 with a series of layers 4504 which are held together at the connecting point 4505.

In another embodiment, the airway implant device with the connecting element further includes an anode, a cathode, a first inductor, and a controller. The anode and cathode are typically connected to the deformable element. The controller typically comprises a microprocessor which is capable of sensing the opening of the air passageway and controlling the energizing of the deformable element. The deformable element is energized with a power supply. For example, when the deformable element is an electroactive polymer element, the power supply is in electrical communication with the deformable element and is activated by electrical energy from the power supply. The deformable element can be physically connected to the power supply for example with a wire lead or can be connected with an inductive coupling mechanism.

In an additional embodiment, the airway implant device with the connecting element further includes a sensor, as described herein. The sensor element is capable of monitoring a condition of an airway to determine likelihood of an apneic event. The condition being monitored is an air passageway gap, air flow pressure, and/or wall tension. The sensor can also provide feedback to modulate the opening of the air passageway by the deformable element.

The airway implant device with a connecting element further includes in some embodiments a non-implanted portion. Preferably the non-implanted portion is in the form of a strip and is used to control the deformable element. Typically this strip includes a power supply and a second inductor, the second inductor capable of interacting with a first inductor.

The connecting element can be used for implanting and/or for retrieving the deformable element, in addition to providing support to the organ being controlled by the airway implant. After implantation, the connecting element typically extends from deformable element to a rigid structure. The connecting element can include at one end an additional anchoring feature to assist with the anchoring to the rigid structure. The connecting element is preferably a wire made of nitinol, stainless steel, titanium or a polymer. The connecting element can be made from one or polymers, such as, for example, polyester or polyethylene; one or more superelastic metals or alloys, such as, for example, nitinol; or from resorbable synthetic materials, such as, for example suture material or polylactic acid.

As set forth above, certain embodiments of the present invention are related to an implantable device for stabilizing the tongue during sleeping.

FIG. 46 shows a simplified drawing of an exemplary tongue implant device in accordance with one embodiment of the present invention shown implanted in the tongue. As is shown in FIG. 46, reference number 5001 refers to the tongue; reference number 5002 refers to mandibula; reference number 5003 refers to the anchoring screws; reference number 5004 refers to an anchoring bracket; reference number 5005 refers to the power or actuation module; reference number 5006 refers to a flexible member, which in one embodiment can be a helix-shaped structure; reference number 5007 refers to the base of the tongue; and reference number 5008 refers to the anchor which can be an absorbable anchor.

As is shown in FIG. 46, the tongue implant can have three sections, namely: i) a proximal section that houses the powering mechanism 5005, the actuation mechanism 5005 and the anchoring mechanism 5004 to the patient's mandibula, ii) a middle flexible section 5006 that links the actuation mechanism 5005 to the distal anchor 5008, and iii) a distal anchor 5008, which can be an absorbable anchor, that allows the implant to be anchored to the base of the tongue 5008. The implant can be placed such that its proximal portion is anchored to the mandibula 5002 and its distal portion is anchored to the base of the tongue 5007.

The Powering/Actuation portion 5005 and its housing can be anchored to the mandibula via a titanium bracket 5004 and titanium bone screws. The actuation mechanisms 5005 can include a Nitinol (actuator type) superelastic shape memory alloys, piezoelectric actuators, and/or electro active polymers, described below in further detail.

The actuator 5005 can be connected to the distal section via a flexible portion 5006 that in one embodiment can be made out of the same actuator material. Alternatively the middle flexible portion 5006 can be made from stainless steel, aramid fiber, polypropylene, nylon or any other suitable material. The flexible portion 5006 can also include a hyaluronic acid (HA) coating to prevent tissue in-growth.

The distal anchor 5008 can be made out of absorbable polymers such as polylactic acid, polyglycolic acid, and so on. Such materials would allow for better integration and anchoring of the implant at the base of the tongue muscle.

FIG. 47 shows a photograph of an exemplary prototype tongue implant device in accordance with one embodiment of the present invention. Shown in FIG. 47 are the leads 5010 for powering the implant, the power/actuation portion 5012, the flexible middle section 5014 and the distal anchor 5016. It should be noted that the simple prototype device shown in FIG. 47 is for testing purposes and thus the novel implant device is not limited to the prototype of FIG. 47.

FIG. 48 shows a simplified schematic drawing of an exemplary tongue implant device in accordance with another embodiment of the present invention. As shown in FIG. 48, the implant can include an anchor portion 5020 for securing the implant to the mandibula; a control portion 5022 for controlling the flexible portion 5024; a flexible portion 5024 and an anchor 5026 for securing the implant to the base of the tongue. As shown in FIG. 48, the actuation mechanism 5022 includes a small linear motor 5025 that is used to provide the linear actuation. For this purpose a Squiggle motor manufactured by New Scale Technologies can be used, but other suitable linear motors may also be used. Alternatively, in other embodiments, instead of motors other mechanisms such as smart active polymers/structures can also be used. As is shown in FIG. 48, the motor 5025 can be anchored to a titanium casing 5023 by using a combination of biocompatible epoxy and mechanical screw type anchoring through an internal anchoring mechanism 5027. The device of FIG. 48 can also have a guide mechanism 5028 which also incorporates a spring preload 5030. In operation, the motor 5025 pushes against a stainless steel block 5032 which is guided by the thin guide rails 5028. One or more springs 5030 can provide the pre-load against a fixed internal part 5029, such that under no load condition the motor shaft has an axial load to displace linearly. The power transmission system 5021 can be attached on top of the titanium casing such that it can be as close to the outside of the chin as possible to effect an inductive power coupling. The titanium casing 5023 has two or more tapped holes 5034 for anchoring it with biocompatible screws to the mandibula.

The tongue stabilizing mechanism or the middle flexible portion 5024 provides for three-dimensional flexibility for the implant. When powered the flexible portion is stiffened along the central longitudinal axis to hold the tongue in position so as not to block the airway. When not powered, the middle flexible portion 5024 provides for three-dimensional flexibility for the implant, so as to enable the patient to have adequate tongue movement during speaking and swallowing. The middle flexible portion 5024 can include a flexible spring, bellows, etched stent or a combination of the three as the mechanism for supporting the tongue. The middle flexible portion can be coated with an HA coating for preventing tissue in-growth. An important functionality of this mechanism is to permit flexible movement of the tongue in all degrees of freedom during its non active (e.g. non-powered) state. And when the actuator is active, it can tighten the tongue and stabilize it, preventing its multiple degrees of freedom. A tough but flexible material such as a Kevlar fiber 5044 can be used to connect the moving end of the actuation mechanism 5032 to the end of the stabilizing mechanism such that when the actuator moves back it pulls the fiber and stiffens the spring or bellow. It too can be coated with HA coating for preventing tissue growth.

The anchoring mechanism 5026 can include two concentric polyester discs 5050A-5050B with one 5050A connected with the tongue stabilizing mechanism with suture holes around its circumference. The second disc 5050B can also have suture holes 5056 around its circumference which are concentric with the holes in the first disc. Both discs can be connected by one or more polyester rods with holes 5052 for tissue in-growth. The disc further away from the middle flexible portion can be surgically inserted at the base of the tongue at a depth such that the second disc is in contact with the base of the tongue. The surgically implanted disc 5050B can also have one or more polyester rods with polyester beads 5054 to facilitate good tissue in-growth and hence good anchoring.

The tongue implant device in accordance with the embodiments of the present invention can have may alternative configurations, including one or more of the following described embodiments. In a first embodiment the flexible middle portion 5022 can be actuated by a combination of a piezoelectric actuator and a linear motor coupled with a cable to stiffen a spring or bellow structure. In a second embodiment, the flexible middle portion 5022 can be actuated by a combination of a Nitinol or other shape memory material obviating the need for a linear motor and cable arrangement. In a third embodiment, the flexible middle portion 5022 can be actuated by combination of an electro active polymer such as polypyrrole, obviating the need for a linear motor and cable arrangement. Preferably, the Nitinol or the polypyrrole material are of a non-toxic medical grade type. Alternatively, the non-medical grade implant materials are encased or coated in medical grade materials. Such coatings can include a hyaluronic acid, or a poly-Lysine acid coating. The power source for the actuation of the implant device can be a non-implanted power source that is inductively coupled with the power-actuation portion of the tongue implant.

FIG. 49 is a simplified schematic drawing of an exemplary tongue implant device 5100 in accordance with another embodiment of the present invention. FIG. 49 is shown as a longitudinal sectional drawing to better show the interior of the implant 5100. The implant 5100 includes a bracket portion 5102 configured to be attached with the mandible. As is shown in FIG. 49 the bracket portion 5102 includes a plurality of apertures that render the bracket 5102 more flexible so as to be bent into a shape that is suitable for attaching the bracket 5102 with a patient's mandible. The bracket 5102 can be an off-the shelf titanium or stainless steel bracket that are non-magnetic in nature. A housing portion 5104 is connected at the distal end of the bracket 5102. The housing 5104 holds the actuation member 5106 for the deformable or the flexible portion 5108 of the implant 5100. The housing 5104 can be made from a ceramic, a nylon, or a polymeric material such a polyphenylene sulfide (PPS). The housing 5104 serves to insulate and isolate the internal actuation member 5106 from the tongue tissue. The actuation member 5106 is a Nitinol actuator, or other shape memory actuator material, formed to have a helical shape. The Nitinol actuator is powered from the leads located at the proximal end 5107 of the actuation member 5106 using an inductively coupled power source as described above. The actuation member 5106 can be in the form of a double or triple or more helical members. The actuation member 5106 is insulated to avoid its forming a short circuit by making contact with itself when powered. The actuation member 5106 can be connected in parallel so as to have only two wires leading back to the proximal end 5107 of the actuation member 5106. The actuation member 5106 is thermally activated by the resistive heating induced by an electric current flow. When the actuation member 5106 is activated, it heats up and contracts. When the actuation member 5106 is deactivated, it will cool down and relax back to its non-contracted state. This contraction/expansion of the actuation member 5106 is harnessed to act on flexible fiber 5110. The fiber 5110 is connected at its proximal end with the distal end of the actuation member 5106. The fiber 5110 is connected at its distal end with an end portion of the deformable portion 5108. Fiber 5110 can be a Kevlar fiber, or any other suitable non-conducting material.

The distal end of the deformable portion 5110 is connected with an anchor member 5112. The anchor 5112 need not be located at the distal end of the deformable portion 5110; it can be located at any length along the deformable portion. The anchor 5112 can be made from an absorbable material. The anchor 5112 is shown to have two sets of anchoring members 5113 and 5114. The distal anchoring member 5113 is configured to prevent an unintended insertion of the implant beyond the desired location, which could cause an exposure of the implant into the oral cavity. The anchor 5112 is also configured to be deployable using a suitable deployment sheath, such a deployment sheath having peal-away portions. Distal tip 5115 is configured have a rounded and narrow shape to render the implant more easily deployable. The anchor 5112 shown in FIG. 49 is an exemplary one and other anchoring configurations, such as those described above can also be employed. In addition, the anchor 5112 and members 5113 and 5114 can be perforated members to help induce a fibrosis if need be. FIG. 50 illustrates the overall appearance of the implant 5100 of FIG. 49.

When the actuation member 5106 is activated, it will pull on fiber 5110 and reduce the flexibility of the deformable member 5108. The tongue stabilizing mechanism or the middle flexible portion 5108 provides for three-dimensional flexibility for the implant. When powered the flexible portion is rendered less flexible along the central longitudinal axis to hold the tongue in position so as not to block the airway. When not powered, the middle flexible portion 5108 provides for three-dimensional flexibility for the implant, so as to enable the patient to have adequate tongue movement during speaking and swallowing. The middle flexible portion can be coated with an HA coating for preventing tissue in-growth. An important functionality of this mechanism is to permit flexible movement of the tongue in all degrees of freedom during its non active (e.g. non-powered) state. And when the actuator is active, it can stabilize the tongue, preventing its multiple degrees of freedom. The implant 5100 can be placed such that its proximal portion is anchored to the mandibula 5002 and its distal portion is anchored to the base of the tongue 5007. The components located inside the housing can all be coated to render them more easily slidable inside the housing during the activation and deactivation of the implant.

FIGS. 51A-D illustrate one exemplary procedure for the placement of the tongue implant. In FIG. 51A, tongue tissue is dissected to make room in the form of a tongue cavity for the implant. FIG. 51B shows that the implant along with a peal-away introducer is inserted into the created cavity. FIG. 51C shows that introducer is pulled back and away. The removal of the sheath deploys the implant. FIG. 51D. shows that in a last step, the bracket in the implant is anchored to the mandible.

Certain aspects of the tongue implant device are directed to a securing or latching mechanism to securely hold the fiber 5110. The latching mechanism will enable the tongue implant to function without needing to be continually powered or activated. In one embodiment, the latching mechanism is configured to be normally closed, in other words the latch is closed when the implant is not powered. The closed latch hold the fiber 5110. As described above, when the implant is powered by either the Nitinol actuator or the linear motor actuator or by way of any of the other actuators described above, a pulling force is imparted on the fiber that runs along the inside of the deformable section so as to reduce the deformable member's flexibility along its axial length. For the implant to remain in this mode, the pulling force needs to be maintained. One way of doing this requires the activation force to be constantly applied by way of constantly powering the implant. Another and more efficient way requires that the pulling force be maintained without having to continually power the implant. The function of the latch mechanism is to enable this functionality. In this normally closed configuration, when the implant is not powered and its deformable portion is in its less flexible mode, the normally closed latch will keep the implant in this less flexible mode. When the implant is powered to transition to its less flexible mode, first the latch is opened to allow the fiber to undergo a pulling action. Then once the flexible portion has completed its transition to its less flexible mode, the implant is unpowered. The unpowering will reset the latch to its closed position and thus maintain the implant in its less flexible mode. The latch mechanism can be made to be coupled with the housing portion. Further details of the operation of the latch mechanism are described below.

FIG. 52 illustrates one embodiment of the latch mechanism 5200. This embodiment of the latch mechanism 5200 includes a retaining member 5206 coupled with the fiber 5110. In the normally closed position, retainer ring 5204 is held against the retaining member 5206 to prevent the fiber 5110 from moving. When powered, the Nitinol wire or coil 5202 which is connected with the retainer ring 5204 is energized and thus pulls the retainer ring 5204 open allowing the retaining member 5206 and thus the fiber 5110 to move.

FIG. 53 is a simplified drawing illustrating an exemplary tongue implant device 5100 in accordance with another embodiment of the present invention (the proximal bracket or anchor portion 5102 is not shown). The implant 5100 includes a housing portion 5104 that houses the actuation and latching mechanisms. The housing portion 5104 is connected at its distal end with the deformable portion 5108. As described above in connection with FIG. 49, the deformable portion 5108 is connected with the anchor 5112 having a distal anchor portion 5115 and a proximal anchor portion 5114. The implant shown in FIG. 53 includes two Nitinol activation coils. A first Nitinol coil 5302 is connected at its distal end with cable or fiber 5304. The fiber 5304 extends through a hollow collet 5306 to the distal end of the deformable member 5108. The activation or powering of first Nitinol member 5302 causes a pulling action on fiber 5304 which will render the deformable member 5108 less flexible along its longitudinal axis. A second Nitinol coil 5322 is connected at its distal end with cable or fiber 5324. The fiber 5324 is connected at its distal end with the proximal end of the collet 5306. The collet 5306 has a conical distal portion 5308 which is split into 2 or more (e.g. 3 or 4) portions which are dimensioned to securely hold the fiber 5304 when the distal portion 5308 is held against the complementarily-shaped conical recess in collet holder 5310. The collet holder 5310 can have a recess at its distal end dimensioned to receive the deformable section 5108. The collet 5306 is spring-biased by the collet spring 5312. Collet spring 5312 is held in its biased position at its proximal end by resting against the housing shoulder 5313 and at its distal end by resting against collet shoulder 5315. The activation of the second Nitinol coil 5322 causes a pulling action on the collet 5306, lifting the collet's distal portion 5306 up and out of the distal end of the complementarily-shaped conical recess in collet holder 5310, thus allowing the first fiber 5304 to be released from the collet's secure hold. Housing 5104 also includes collet guide portion 5326. The collet guide portion 5326 of the housing 5104 is dimensioned to act as a bearing for the collet and thus guide the collet during its movement. In addition, the collet guide portion 5326 of the housing 5104 has a groove that is dimensioned to receive a complementarily-shaped key in the collet to also guide the movement of the collet 5306 in the housing 5104 and to prevent the rotation of the collet with respect to the housing and to prevent the tangling of the two Nitinol members 5302 and 5322 during the operation of the implant. Alternatively, the collet guide portion 5326 of the housing 5104 can have a key that is dimensioned to receive a complementarily-shaped groove in the collet to also guide the movement of the collet 5306 in the housing 5104 and to prevent the rotation of the collet with respect to the housing.

The sequence of operation for placing the implant of FIG. 53 in its active mode is as follows. First the collet latch mechanism is activated to move and keep it in the unlocked position. Then the fiber pull mechanism is activated until sufficient flexibility in the deformable member has been removed. Then the latch mechanism is unpowered to have it return the collet to its spring-biased locked position. Then once the collet latch is in its normally closed position, the fiber pull mechanism is unpowered. The above sequence of operation is also applicable to the retaining member and retainer ring latch mechanism.

The sequence of operation for placing the implant of FIG. 53 in its non-active mode is as follows. The latch mechanism is activated to move and keep it in the unlocked position. Then a subsequent tongue movement will extend and impart a slack to the fiber, returning the deformable portion to its deformable and flexible mode. The above sequence of operation is also applicable to the retaining member and retainer ring latch mechanism.

FIG. 54 is an exploded assembly view corresponding to the implant of FIG. 53. FIG. 55A illustrates the collet latch in its normally-closed position, and FIG. 55B shows the collet latch in its open position. The upward movement of the collet to its open position is arrested by the mating of the collet's proximal end against the shoulder portion 5328 of the housing. The housing, collet and collet holder can all be made from medical grade plastic materials and they can be coated with HA coating for preventing tissue in-growth.

FIG. 56 is a graph showing the performance characteristic for the shape memory actuator material used in the tongue implant. The shape memory material can be a shape memory alloy with a temperature-dependant phase transformation. The temperature at which the shape memory material changes its crystallographic structure, called transformation temperature, is characteristic of the alloy, and can be tuned by varying the elemental ratios in the alloy. This tuning of the transition temperature is known to those skilled in art and is disclosed in several issued U.S. patents, including for example U.S. Pat. Nos. 3,558,369; 4,310,354; and 4,505,767, the disclosures of which are hereby incorporated by reference herein. The shown performance characteristic of FIG. 56 will be recognized as a material specification to those skilled in the art. In FIG. 56, the X-axis refers to the temperature in Deg. C. and the Y-axis refers to the percent Austenite or percent Martensite. A_(s) refers to the starting point for the change of phase from the martensitic phase to the austenitic phase. A_(f) refers to the point at which the change of phase from the martensitic phase to the austenitic phase has been completed. M_(s) refers to the starting point for the change of phase to the martensitic phase from the austenitic phase, and M_(f) refers to the point at which the change of phase from the austenitic phase to the martensitic phase has been completed. As can be seen in FIG. 56, the key phase transition points are as follows: A_(s) is approximately equal to 47° C.; A_(f) is approximately equal to 60° C.; M_(s) is approximately equal to 52° C., and M_(f) is approximately equal to 42° C. The above-mentioned transition temperatures can have a variation of ±2° C.

The operation of the shape memory actuator material in the tongue implant, starting from a nonpowered state is as follows. With the implant in the nonpowered state, the flexible portion of the implant is in it most flexible state. In this flexible state, the shape memory actuator and the implant are in thermal equilibrium with the body of the patient and thus are at approximately 37° C. Even in a patient experiencing high fever conditions (e.g. about 42° C.), the shape memory actuator material is still in its martensitic (uncontracted state). Once the device is powered, the resistive heating of the shape memory actuator material will cause its temperature to begin to rise, initially approaching A_(s) and continuing to A_(f). The transition in phase from the martensitic to the austenitic phase induced by the resistive heating of the shape memory actuator material will cause a pulling action on the flexible fiber and hence reduce the flexibility of the flexible portion of the implant. The transition time from the martensitic to the austenitic phase can take as long as a few minutes, but is most typically less than 2 minutes. The transition time can also be made extremely small by having an increase in the rate of current flow and its resulting resistive heating. Of course, a desired transition time will take patient comfort into account. The activated implant can then be held in place by the operation of the latch mechanism as described above. The latch mechanism also uses a shape memory actuator material that has the characteristic shown in FIG. 56. The use of the latch mechanism allows the implant to be in its less flexible state without the need to continuously power the implant. The continuous powering of the implant could cause a slight discomfort for the patient due to the warmer temperature of the shape memory actuator material in its contracted state. Accordingly, for a continuously powered implant the thermal insulating properties of the housing would require further consideration to minimize potential patient discomfort. In addition, the thermal insulation for the housing needs to be sufficiently low so as to not impede the cooling of the shape memory actuator material upon unpowering the implant. By not resistively heating the shape memory material actuator, it will cool down to M_(s) and begin its transition back to M_(f). The unheated or non-contracted shape memory material actuator does not impart a pulling force on the flexible portion of the implant. Likewise the unheated or non-contracted shape memory actuator material does not provide an opening force to the normally-closed latch mechanism.

The performance characteristic for the shape memory actuator material used in the tongue implant in accordance with FIG. 56 is advantageous for several reasons. First, the transition from the martensitic to the austenitic phase occurs at a temperature range that is above a patient's normal body temperature. This is advantageous because it insures that the device does not get inadvertently activated, for example by a patient experiencing a high fever, or by a patient drinking a hot beverage. In addition, the inadvertent activation is also prevented by the presence of the latch mechanism. Second, the transition from the martensitic to the austenitic phase occurs over a rather narrow temperature range (e.g., less than 20° C.). This insures an effective implant operation in the expected range of temperatures; the implant does not get inadvertently activated, and the implant will remain in its non-activated state in a patient having a normal body temperature range. The normal body temperature as used herein includes a patient experiencing chilled (e.g. in an operating room) or an elevated temperature (e.g. fever). Furthermore, the temperature range for the transition from the martensitic to the austenitic phase and back insures that the implant will have a high fatigue rating, insuring that the implant will have an adequate operational life.

Methods of Making Electroactive Polymer Element

In some embodiments, the EAP element is an IPMC strip which is made from a base material of an ionomer sheet, film or membrane. The ionomer sheet is formed using ionomer dispersion.

IPMC is made from the base ionomer of, for example, polyethylene, polystyrene, polytetrafluoroethylene, polyvinylidene fluoride (PVDF) (e.g., KYNAR® and KYNAR Flex®, from ATOFINA, Paris, France, and SOLEF®, from Solvay Solexis S.A., Brussels, Belgium), hydrophilic-PVDF (h-PVDF), polyfluorosulfonic acid based membranes like NAFION® (from E.I. Du Point de Nemours and Company, Wilmington, Del.), polyaniline, polyacrylonitrile, cellulose, cellulose acetates, regenerated cellulose, polysulfone, polyurethane, and combinations thereof. The conductive material that is deposited on the ionomer can be gold, platinum, silver, palladium, copper, graphite, conductive carbon, or combinations thereof. Conductive material is deposited on the ionomer either by electrolysis process, vapor deposition, sputtering, electroplating, or combination of processes.

The IPMC is cut into the desired implant shape for the EAP element. The electrical contact (e.g., anode and cathode wires for EAP element) is connected to the IPMC surfaces by, for example, soldering, welding, brazing, potting using conductive adhesives, or combinations thereof. The EAP element is configured, if necessary, into specific curved shapes using mold and heat setting processes.

In some embodiments, the EAP element is insulated with electrical insulation coatings. Also, the EAP element can be insulated with coatings that promote cell growth and minimize fibrosis, stop cell growth, or kill nearby cells. The insulation can be a biocompatible material. The EAP element is coated with polymers such as polypropylene, poly-L-lysine, poly-D-lysine, polyethylene glycol, polyvinyl alcohol, polyvinyl acetate, polymethyl methacrylate, or combinations thereof. The EAP element can also be coated with hyaluronic acid. The coating is applied to the device by standard coating techniques like spraying, electrostatic spraying, brushing, vapor deposition, dipping, etc.

In one example, a perfluorosulfonate ionomer, PVDF or h-PVDF sheet is prepared for manufacturing the EAP element. In an optional step, the sheet is roughened on both sides using, for example, about 320 grit sand paper and then about 600 grit sand paper; then rinsed with deionized water; then submerged in isopropyl alcohol (IPA); subjected to an ultrasonic bath for about 10 minutes; and then the sheet is rinsed with deionized water. The sheet is boiled for about 30 minutes in hydrochloric acid (HCL). The sheet is rinsed and then boiled in deionized water for about 30 minutes. The sheet is then subject to ion-exchange (i.e., absorption). The sheet is submerged into, or otherwise exposed to, a metal salt solution at room temperature for more than about three hours. Examples of the metal salt solution are tetraammineplatinum chloride solution, silver chloride solution, hydrogen tetrachloroaurate, tetraamminepalladium chloride monohydrate or other platinum, gold, silver, carbon, copper, or palladium salts in solution. The metal salt solution typically has a concentration of greater than or equal to about 200 mg/100 ml water. 5% ammonium hydroxide solution is added at a ratio of 2.5 m/1000 ml to the tetraammineplatinum chloride solution to neutralize the solution. The sheet is then rinsed with deionized water. Primary plating is then applied to the sheet. The sheet is submerged in water at about 40° C. 5% solution by weight of sodium borohydride and deionized water is added to the water submerging the sheet at 2 ml/180 ml of water. The solution is stirred for 30 minutes at 40° C. The sodium borohydride solution is then added to the water at 2 ml/180 ml of water and the solution is stirred for 30 minutes at 40° C. This sodium borohydride adding and solution stirring is performed six times total. The water temperature is then gradually raised to 60° C. 20 ml of the sodium borohydride solution is then added to the water. The solution is stirred for about 90 minutes. The sheet is then rinsed with deionized water, submerged into 0.1N HCI for an hour, and then rinsed with deionized water.

In some embodiments, the sheet receives second plating. The sheet is submerged or otherwise exposed to a tetraammineplatinum chloride solution at a concentration of about 50 mg/100 ml deionized water. 5% ammonium hydroxide solution is added at a rate of 2 ml/1100 ml of tetrammineplatinum chloride solution. 5% by volume solution of hydroxylamine hydrochloride in deionized water is added to the tetraammineplantium chloride solution at a ratio of 0.1 of the volume of the tetraammineplatinum chloride solution. 20% by volume solution of hydrazine monohydrate in deionized water is added to the tetraammineplatinum chloride solution at a ratio of 0.05 of the volume of the tetraammineplantinum chloride solution. The temperature is then set to about 40° C. and the solution is stirred.

A 5% solution of hydroxylamine hydrochloride is then added at a ratio of 2.5 m/100 ml of tetraammineplatinum chloride solution. A 20% solution of hydrazine monohydrate solution is then added at a ratio of 1.25 ml/100 ml tetraammineplatinum chloride solution. The solution is stirred for 30 minutes and the temperature set to 60° C. The above steps in this paragraph can be repeated three additional times. The sheet is then rinsed with deionized water, boiled in HCl for 10 minutes, rinsed with deionized water and dried.

In some embodiments, the polymer base is dissolved in solvents, for example dimethyl acetamide, acetone, methylethyle ketone, toluene, dimethyl carbonate, diethyl carbonate, and combinations thereof. The solvent is then allowed to dry, producing a thin film. While the solution is wet, a low friction, (e.g., glass, Teflon) plate is dipped into the solution and removed. The coating on the plate dries, creating a think film. The plate is repeatedly dipped into the solution to increase the thickness of the film.

Polyvinyl alcohol, polyvinyl pyrrolidone, polyinyl acetate or combinations thereof can be added to a PVDF solution before drying, thus contributing hydrophilic properties to PVDF and can improve ion migration through the polymer film during manufacture. Dye or other color pigments can be added to the polymer solution.

Method of Using

FIG. 25 illustrates an embodiment of a method of the airway implant device of the present invention. In this embodiment, the first inductor 18 is implanted in the mouth roof 72, for example in or adjacent to the hard palate 74. Wire leads 6 connect the first inductor 18 to the deformable elements 8 a, 8 b, and 8 c. A first deformable element 8 a is implanted in the base of the tongue at the pharynx wall 76. A second deformable element 8 b is integral with the first deformable element 8 a (e.g., as two sections of a hollow cylindrical deformable element 8, such as shown in FIG. 17). The first and second deformable elements 8 a and 8 b can be separate and unattached elements. The third deformable element 8 c is implanted in the uvula and/or soft palate 84. The deformable elements 8 can also be implanted in the wall of the nasal passages 78, higher or lower in the pharynx 79, such as in the nasal pharynx, in the wall of the trachea 80, in the larynx (not shown), in any other airway, or combinations thereof. The second inductor 16 is worn by the patient in the mouth 82. The second inductor 16 is connected to an integral or non-integral power supply. The second inductor 16 comprises one or multiple induction coils. The second inductor 16 inductively transmits RF energy to the first inductor 18. The first inductor 18 changes the RF energy into electricity. The first inductor 18 sends a charge or current along the wire leads 6 to the deformable elements 8 a, 8 b, and 8 c. The deformable elements 8 a, 8 b, and 8 c are energized by the charge or current. The energized deformable elements 8 a, 8 b, and 8 c increase the stiffness and/or alter the shape of the airways. The energized deformable elements 8 a, 8 b, and 8 c modulate the opening of the airways around which the deformable elements 8 a, 8 b, and 8 c are implanted. The non-energized deformable elements 8 a, 8 b, and 8 c are configured to conform to the airway around which the deformable elements 8 a, 8 b, and 8 c are implanted. The non-energized deformable elements 8 a, 8 b, and 8 c are flexible and soft.

FIG. 26 illustrates another embodiment of the invention. In this embodiment, the first inductor 18 is implanted in the mouth roof 72 and attached to a deformable element 8 via the wire lead 6. The deformable element 8 is preferably in the soft palate 84. In another embodiment, FIG. 27 illustrates that the first inductor 18 is implanted in the mouth roof 72 and attached to two deformable elements 8 via two wire leads 6. The deformable elements 8 are implanted in side walls 86 of the mouth 82. In yet another embodiment, as illustrated in FIG. 28, the first inductor 18 is implanted in the mouth roof 72 and attached to three deformable elements 8 via three wire leads 6. The deformable elements 8 are implanted in the soft palate 84 and the side walls 86 of the mouth 82. FIG. 29 illustrates an embodiment in which the first conductors (not shown, e.g., the tooth sockets), are attached to, and in conductive electrical communication with, the second conductors. The retainer 66, such as shown in FIG. 23, can be worn by the patient to energize the deformable element 8. The tooth sockets are removably attached to the first conductors 34. The first conductors 34 are dental fillings, conductive posts adjacent to and/or through the teeth 64.

FIG. 33 illustrates an embodiment in which a patient 88 has the first transducer (not shown) implanted in the patient's cheek and wears the non-implanted portion 22, such as shown in FIG. 24, on the outside of the patient's cheek. The non-implanted portion 22 energizes the implanted portion (not shown).

FIGS. 34-36 depict some of the ways in which the implant devices function to open the airways. FIGS. 34A and 34B depict a side view of a patient with a soft palate implant 8 c and a non-implanted portion of the device, with a second inductor 16, which in this case is a wearable mouth piece. The wearable mouth piece includes a transmitter coil, a power source, and other electronics, which are not depicted. Also, shown is a first inductor 18. The implant device has the ability to sense and deflect the tongue so as to open the airway. FIG. 34A depicts the tongue 92 in its normal state. During sleep, when the tongue collapses 92′, as shown in FIG. 34B, the deformable element 8 c′ senses the collapsed tongue and is energized via the mouthpiece and first inductor and it stiffens to push away the tongue from the airway and keeps the airway open. This opening of the airway can be partial or complete. In some embodiments, particularly the embodiments without the sensor, the implant is powered when the patient is asleep such that the deformable element 8 is energized and keeps the collapsed tongue away from the airway.

FIGS. 35 and 36 depict an embodiment of keeping the airways open with lateral wall implants. FIG. 35A shows a side view of a patient's face with a deformable element 8 located in the lateral wall of the airway. FIG. 35A depicts the tongue 92 in its normal state. FIG. 35B depicts the tongue 92′ in a collapsed state. When the tongue is in this state or before it goes into the collapsed state the deformable element 8 is energized so as to stretch the lateral walls and open the airway, as shown in FIG. 36B. FIGS. 36A and 36B are a view of the airway as seen through the mouth of patient. FIG. 36 A depicts the deformable elements 8 in a non-energized state and the tongue in a non-collapsed state. When the tongue collapses or it has a tendency to collapse, such as during sleep, the deformable element 8 is energized and airway walls are pushed away from the tongue and creates an open air passageway 93. This embodiment is particularly useful in obese patients.

Airway Diseases

During sleep, the muscles in the roof of the mouth (soft palate), tongue and throat relax. If the tissues in the throat relax enough, they vibrate and may partially obstruct the airway. The more narrowed the airway, the more forceful the airflow becomes. Tissue vibration increases, and snoring grows louder. Having a low, thick soft palate or enlarged tonsils or tissues in the back of the throat (adenoids) can narrow the airway. Likewise, if the triangular piece of tissue hanging from the soft palate (uvula) is elongated, airflow can be obstructed and vibration increased. Being overweight contributes to narrowing of throat tissues. Chronic nasal congestion or a crooked partition between the nostrils (deviated nasal septum) may be to blame.

Snoring may also be associated with sleep apnea. In this serious condition, excessive sagging of throat tissues causes your airway to collapse, preventing breathing. Sleep apnea generally breaks up loud snoring with 10 seconds or more of silence. Eventually, the lack of oxygen and an increase in carbon dioxide signal causes the person to wake up, forcing the airway open with a loud snort.

Obstructive sleep apnea occurs when the muscles in the back of the throat relax. These muscles support the soft palate, uvula, tonsils and tongue. When the muscles relax, the airway is narrowed or closed during breathing in, and breathing is momentarily cut off. This lowers the level of oxygen in the blood. The brain senses this decrease and briefly rouses the person from sleep so that the airway can be reopened. Typically, this awakening is so brief that it cannot be remembered. Central sleep apnea, which is far less common, occurs when the brain fails to transmit signals to the breathing muscles.

Thus, it can be seen that airway disorders, such as sleep apnea and snoring, are caused by improper opening of the airway passageways. The devices and methods described herein are suitable for the treatment of disorders caused by the improper opening of the air passageways. The devices can be implanted in any suitable location such as to open up the airways. The opening of the passageways need not be a complete opening and in some conditions a partial opening is sufficient to treat the disorder.

In addition to air passageway disorders, the implants disclosed herein are suitable for use in other disorders. The disorders treated with the devices include those that are caused by improper opening and/or closing of passageways in the body, such as various locations of the gastro-intestinal tract or blood vessels. The implantation of the devices are suitable for supporting walls of passageways The devices can be implanted in the walls of the gastro-intestinal tract, such as the esophagus to treat acid reflux. The gastro-intestinal tract or blood vessel devices can be used in combination with the sensors described above. Also, the implants and/or sphincters can be used for disorders of fecal and urinary sphincters. Further, the implants of the invention can be tailored for specific patient needs.

Methods and Devices for Removal

FIG. 57A is a simplified schematic drawing of an exemplary tongue implant device 6000 in accordance with another embodiment of the present invention. The implant device 6000 is largely as described as in FIGS. 49 and 50, and thus may share an almost identical construction. The implant device 6000 may also share the basic construction of any of the implant devices disclosed herein. As disclosed above, the implant includes a housing 5104 holding an actuation member (not shown), a flexible portion 5110 (also known as the flexible fiber), anchor 5112, distal tip 5115, and a bracket portion 5102 configured to be attached with the mandible. The implant device 6000 differs from other implant devices disclosed herein in that an additional suture member 6002 is included. The suture member 6002 is shown in interwoven about at least a portion of the anchor 5112, for example around anchor member 5114. The suture member 6002 may be interwoven about the anchor member 5114 such that when pulled in a proximal direction (e.g. towards the mandible) the anchor members 5114 will collapse. The suture member 6002 may be interwoven in a slipknot fashion around each anchor member 5114, thus configured to apply an even and simultaneous pulling force around each anchor member 5114. Each anchor member 5114 may also include individual suture members 6002. One suture member 6002 is shown, with two ends 6004 in the proximal area of the implant device 6000, however, only one end 6004 is required. The suture member 6002 may be intended to be utilized when the implant device 6000 is required to be removed from a patient, for example due to improper placement or infection. Collapsing the anchor member 5114 allows the implant device 6000 to be moved in a proximal or distal direction, without the anchor member 5114 dragging or catching on tissue. The suture member 6002 may be constructed from a biodegradable, e.g. bioabsorbable, material, such as polylactic acid or polylactide (PLA). Thus after an appropriate amount of time, e.g. 1-12 months, the suture member 6002 may absorb into a patient's body. An optional cap 6006 is also shown covering the distal anchoring member 5113. The cap 6006 is utilized to allow the implant device to be pushed in a distal direction without impediment from the distal anchoring member 5113 dragging or catching on tissue. Thus when a removal technique is utilized, which requires the implant device 6000 to be moved in a distal direction, the cap 6006 allows positive movement and removal. The cap 6006 may be constructed from a biodegradable, e.g., bioabsorbable, material such as polylactic acid or polylactide (PLA). Thus after an appropriate amount of time, e.g., 1-12 months, the cap 6006 may absorb into a patient's body. The cap 6006 is shown as transparent to aid in discussion of the figure, but also may be opaque or solid.

FIGS. 57B-57E show a method for removing a previously implanted device from a patient's tongue, according to one embodiment of the invention. The method may be practiced after a relatively long period of time after implantation of the device has occurred, e.g., after tissue in-growth into portions of the device has occurred. An implanted device 6000, for example as shown in FIG. 57A, is shown in a cross-section of a patient's tongue. However, this method may be implemented regarding any of the implanted devices disclosed herein. The anchor member 5114 and distal anchor member 5113 are shown anchored in the base of the tongue T. The suture member 6002 is also shown extending past the housing 5104. A first incision I1 is made under the chin area to expose the mandible M and implanted device 6000.

In FIG. 57C, the bracket portion 5112 (not shown) has been disconnected or detached from the mandible, and the housing 5104 (not shown) has been cut or cleaved from the flexible portion 5110 and removed through the first incision I1. The suture member 6002 (not shown) also has been pulled in a distal direction, e.g., towards the first incision I1, to remotely collapse the anchor member 5114, now 5114C. Thus the collapsed anchor member 5114C will not inhibit distal or proximal movement of the remaining portion of the implanted device 6000. Alternatively, a clamping device (not shown) may be used in lieu of, or in conjunction with, the suture member 6002 to remotely collapse the anchor member 5114.

In FIG. 57D a cannula-based removal device 6010 is advanced through the first incision I1. A suture (not shown) may be tied or affixed to the flexible portion 5110 before the removal device is inserted. The suture (not shown) may thus be used as an aid for removal. The removal device 6010 includes a snare 6012 for grasping onto the suture (not shown) or the remaining portion of the flexible portion 5110. The snare 6012 applies a tension onto the suture (not shown) or the remaining portion of the flexible portion 5110, and then the removal device 6010 may be advanced towards the direction of the tongue base T. The removal device 6010 continuously applies a tension onto the remaining portion of the implanted device 6000, which positively locks the removal device 6010 with the implanted device 6000, in order to be able to push the implanted device in a distal direction, e.g. towards the tongue base T. A locking mechanism (not shown) may be implemented in a proximal region of the removal device 6010 to lock the snare into a tensioned mode with the implanted device 6000.

In FIG. 57E the removal device 6010 is shown fully advanced onto the implanted device 6000, with a continuous tension applied by the snare 6012. The removal device 6010 may partially or completely advanced over the implanted device 6000, such that the implanted device 6000 is partially or completely within the cannula of the removal device 6010. A second incision 12 is made at a distal portion of the tongue, inside the mouth region which exposes a distal most portion of the implanted device 6000 and the cap 6006. The removal device 6010 may then be pushed distally to expel the distal most portion of the implanted device 6000 into the mouth cavity MC, which may be confirmed visually. The cap 6006 prevents the distal anchoring member 5113 from dragging or catching on tissue. Once the distal most portion of the implanted device 6000 is expelled into the mouth cavity MC, it may be removed conventionally, e.g., with forceps. The removal device 6010 is then removed from the patient and the first and second incisions I1, 12, may be surgically closed.

FIG. 58A is a simplified schematic drawing of an exemplary tongue implant device 6014 in accordance with another embodiment of the present invention. The implant device is largely identical to the implant device 6000 shown in FIG. 57A, however, the implant device 6014 may not include a cap, and additionally includes a sheath 6016. The sheath 6016 aids in removal of the implant device 6014. The sheath 6016 is an elongated tube and covers a majority of the implant device 6014. The sheath may be constructed from a biodegradable, e.g., bioabsorbable, material such as polylactic acid or polylactide (PLA). Thus the sheath acts as a temporary barrier from tissue growing into the implant device 6000.

FIGS. 58B and 58C show a method for removing a previously implanted device from a patient's tongue, according to one embodiment of the invention. The method may be practiced after a relatively short period of time after implantation of the device has occurred, e.g., before tissue in-growth into portions of the device has occurred. An implanted device 6014, for example as shown in FIG. 58A, is shown in a cross-section of a patient's tongue. However, this method may be implemented regarding any of the implanted devices disclosed herein. The anchor member 5114 and distal anchor member 5113 are shown anchored in the base of the tongue. The suture member 6002 is also shown extending past the housing 5104. An incision 13 is made under the chin area to expose the mandible M and implanted device 6014.

In FIG. 58C, the bracket portion 5112 (not shown) has been disconnected or detached from the mandible, and the housing 5104 (not shown) has been cut or cleaved from the flexible portion 5110, or flexible section, and removed through the incision 13. The bracket portion 5112 and the housing 5104 may also be left intact with the flexible portion 5110. The suture member 6002 (not shown) has been pulled in a distal direction, e.g., towards the incision 13, to remotely collapse the anchor member 5114, now 5114C. Thus the collapsed anchor member 5114C will not inhibit distal or proximal movement of the remaining portion of the implanted device 6000. Alternatively, a clamping device (not shown) may be used in lieu of, or in conjunction with, the suture member 6002 to remotely collapse the anchor member 5114. The implanted device 6014 may then be removed or pulled in a proximal direction, e.g., towards the incision 13, to expel the device, for example, by grasping the bracket portion 5112 with forceps and pulling in a proximal direction. The distal anchor member 5113 does not inhibit the proximal removal of the implanted device, because the distal anchor member 5113 is preferentially angled to only inhibit distal movement. A removal device (not shown) may be used to remove the implanted device 6014 if the housing 5104 has been cut or cleaved from the flexible portion 5110. The removal device (not shown) is generally identical in use and construction as the removal device 6010 shown in FIGS. 57D and 57E, however, the removal device (not shown) is used to pull in a proximal direction rather than push in a distal direction. The sheath 6016 allows the implanted device 6014 to be easily removed from the patient, as the sheath 6016 temporarily prevents tissue from growing into or adhering to the implanted device. The sheath 6016 may be removed through the incision 13 after the implanted device 6014 has been removed, and the incision 13 may be surgically closed.

FIG. 59A shows a removal device 6018, according to one embodiment of the invention, and which may be used for example in the methods described in FIGS. 57B-57E, 58B, and 58C. The removal device 6018 includes a cannula 6020, which for example may be constructed from a hypotube. The cannula 6020 may include a beveled tip 6021 which aids in bisecting tissue. The cannula 6020 may be constructed from stainless steel. The cannula 6020 may also be malleable, which allows a user to bend the cannula, in the field, to an optimal bend or angle for a specific patient. The cannula 6020 may also include a curve to aid in positioning the removal device 6018 in an optimum area within the tongue. The removal device 6018 includes a handle 6022 which is attached to the cannula 6020. A moveable snare 6024 may run within the cannula 6020 and the handle 6022. A linear actuator 6026 can move the snare in a distal and proximal direction, to decrease and increase tension on an implanted device, respectively. The linear actuator may be manually or electrically operated. The handle also may include a locking mechanism 6028, which can turn about the working axis of the cannula 6020, as shown. When locked, the locking mechanism 6028 can prevent the snare 6024 from moving in a distal or proximal direction. The locking mechanism 6028 is shown as a separate mechanism from the linear actuator 6026, but this is merely illustrative. The locking mechanism 6028 may be integral with the linear actuator, for example, the locking mechanism 6028 may be implemented as a ratcheting mechanism.

FIG. 59B shows a clamping device 6030 according to one embodiment of the invention, and which may be used, for example, in the methods described in FIGS. 57B-57E and 58B and 58C. The clamping device 6030 is used to collapse a portion of an implant device, for example, the anchor member 5114 and distal anchoring member 5113. The clamping device 6030 includes a clamping mechanism 6032, which for example may use a ratcheting mechanism or screw driven mechanism similar to a hose clamp, or any mechanism which decreases in size or diameter. The clamping mechanism 6032 is attached to an elongated member 6034, which is attached to a handle 6036. The handle 6036 can include an actuator 6038 which may be turned in order to actuate the clamping mechanism 6032. For example, the actuator 6038 may directly or indirectly cause the elongated member 6034 to rotate and thus actuate the clamping mechanism 6032. The clamping device 6030 may be used in lieu of, or in conjunction with, the suture member 6002 to remotely collapse a portion of the anchor 5112. In use, the clamping device 6030 is placed in a position such that the clamping mechanism 6032 surrounds all or a portion of the anchor 5112. The clamping mechanism 6032 is then actuated to decrease in diameter such that all or a portion of the anchor 5112 is crushed or flattened. The clamping mechanism 6032 may then be un-actuated and the clamping device 6030 removed. Alternatively, the clamping mechanism 6032 may be left clamped around the anchor 5112 and used as an aid to remove the implanted device.

As will be understood by those skilled in the art, the present invention may be embodied in other specific forms without departing from the essential characteristics thereof. Those skilled in the art will recognize, or be able to ascertain using no more than routine experimentation, many equivalents to the specific embodiments of the invention described herein. Such equivalents are intended to be encompassed by the following claims. 

1. A method for removing a previously implanted tongue device, the method comprising: making a first incision under the chin area to expose the mandible and the implanted device; detaching a proximal portion of the implanted device at a flexible section of the implanted device, the flexible section connected to an anchor in the tongue base; guiding a portion of the flexible section to a cannula of a removal device which is advanced through the first incision; advancing the cannula towards the tongue base; making a second incision in the tongue base through the oral cavity and above the anchor; pushing the cannula through the second incision made in the tongue base and into the oral cavity; and removing the implanted device from the oral cavity.
 2. The method of claim 1 additionally comprising collapsing at least a portion of the anchor.
 3. The method of claim 2 wherein collapsing is performed using a clamping device.
 4. The method of claim 2 wherein the collapsing is performed by pulling on at least one suture member which is attached to at least a portion of the anchor.
 5. The method of claim 4 wherein, the suture member is bioabsorbable.
 6. The method of claim 1 wherein at least a portion of the anchor is covered by a cap which allows the anchor to be pushed into the oral cavity.
 7. The method of claim 6 wherein the cap is constructed from a biodegradable material.
 8. The method of claim 1 additionally comprising visually confirming the implanted device entering the oral cavity.
 9. The method of claim 1 wherein the cannula of the removal device is a hypotube which is beveled at a distal portion.
 10. The method of claim 1 wherein guiding includes attaching a suture to the flexible section and advancing the suture through the cannula of the removal device.
 11. The method of claim 10 wherein the removal device applies a tension to the suture.
 12. The method of claim 11 wherein the removal device includes a suture grasping mechanism inside the cannula.
 13. The method of claim 12 wherein the suture grasping mechanism includes a loop snare.
 14. The method of claim 1 additionally comprising detaching the portion of a previously implanted tongue implant device from the mandible.
 15. A removable implant for aiding in stabilizing the tongue, comprising: a control portion which attaches to a mandible, the control portion including an actuator; a flexible portion which connects to a control portion and is actuated by the actuator; an anchoring member connected with the flexible portion, the anchoring member being configured to be implanted within a tongue base; and sutures connected to at least a portion of the anchoring member and extending to the control portion, which when pulled collapses at least a portion of the anchoring member.
 16. The removable implant of claim 15 wherein the tongue anchoring portion includes hooks and the sutures are looped around the hooks.
 17. The removable implant of claim 15 additionally comprising a cap positioned about a portion of the anchoring member.
 18. The removable implant of claim 17 wherein the cap is bioabsorbable.
 19. The removable implant of claim 15 additionally comprising a bracket attached to the control portion, and configured to anchor to a mandible.
 20. The removable implant of claim 15 additionally comprising a bioabsorbable sheath surrounding the flexible portion.
 21. The removable implant of claim 15 wherein the sutures are bioabsorbable.
 22. A method for removing a previously implanted tongue implant device, the method comprising: creating an incision about the mandible area where a portion of a previously implanted tongue implant device is attached to the mandible; detaching the portion of a previously implanted tongue implant device from the mandible, the previously implanted tongue device also including anchors secured to the tongue; remotely collapsing at least a portion of the anchors of the previously implanted tongue device; and pulling out the previously implanted tongue device through the incision.
 23. The method of claim 22 wherein the previously implanted tongue implant device is located within a sheath.
 24. The method of claim 23 additionally comprising pulling the sheath out of the incision.
 25. The method of claim 22 wherein collapsing is performed using a clamping device.
 26. The method of claim 22 wherein collapsing is performed by pulling on at least one suture member which is attached to least a portion of the anchor.
 27. The method of claim 25 wherein the suture member is bioabsorbable.
 28. The method of claim 22 additionally comprising inserting a removal device into the incision and using the removal device for pulling out the previously implanted tongue device.
 29. The method of claim 28 wherein the removal device includes a hypotube which is beveled at the distal portion.
 30. The method of claim 28 wherein the removal device snares a portion of the previously implanted tongue implant device.
 31. The method of claim 22 wherein the previously implanted tongue implant device was not implanted for a long enough period for tissue to significantly adhere to the previously implanted tongue implant device. 